Zobrazeno 1 - 10
of 466
pro vyhledávání: '"L. N. YAKHONTOV"'
Study of the metabolism of the new anti-ulcer drug quiditene [(3-quinuclidyl)-di(2-thienyl)carbinol]
Autor:
S. M. Tupikina, Yu. N. Sheinker, L. N. Yakhontov, M. É. Kaminka, O. S. Anisimova, M. V. Polikarpov, E. F. Kuleshova, L. N. Koikov
Publikováno v:
Pharmaceutical Chemistry Journal. 29:26-29
Thin-layer chromatography and mass spectrometry were used to study the metabolism of the new anti-ulcer drug Quiditene. After oral administration in a dose of 100 mg/kg, urine samples taken 2 h later showed no metabolites. Later samples (taken 4, 6,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::039dda03fcc719a0781f370e04654046
https://doi.org/10.1007/bf02219457
https://doi.org/10.1007/bf02219457
Autor:
A. A. Prokopov, L. N. Yakhontov
Publikováno v:
Pharmaceutical Chemistry Journal. 28:471-506
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a04ed44db21e239127d591b8cefb5b5b
https://doi.org/10.1007/bf02219249
https://doi.org/10.1007/bf02219249
Autor:
Yu. N. Sheinker, V. A. Bondarenko, L. N. Yakhontov, T. Ya. Filipenko, K. F. Turchin, E. E. Mikhlina
Publikováno v:
Chemistry of Heterocyclic Compounds. 29:103-108
Proton and carbon-13 NMR spectroscopy have been used to confirm the structure and establish the 4a,7a(RR/SS) configuration of 4a-hydroxyisoxazolidino[4,5-b]quinuclidines obtained by the reaction of N-arylhydroxylamines with 2-methylene-3-oxoquinuclid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63f9aedaa52e3d67fc51c617d980b8f9
https://doi.org/10.1007/bf00528646
https://doi.org/10.1007/bf00528646
Autor:
M. F. Marshalkin, L. N. Yakhontov, Ye. F. Kuleshova, K. F. Turchin, G. P. Zhikhareva, Yu. N. Sheinker
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe5d7124414574f94ac3fd0303a5aad8
https://doi.org/10.1002/chin.199121194
https://doi.org/10.1002/chin.199121194
Autor:
E. V. Lomanova, I. N. Fedorova, Lyudmila M. Alekseeva, M. D. Mashkovskii, K. F. Turchin, V. I. Shvedov, M. Ya. Uritskaya, L. N. Yakhontov, R. G. Glushkov, E. F. Kuleshova, O. A. Fedotova, N. I. Andreeva, N. V. Darinskii, O. R. Arbuzova, P. Yu. Ivanov, V. A. Parshin
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c41c8fcecebdb78243a5e9cbad719a61
https://doi.org/10.1002/chin.199120192
https://doi.org/10.1002/chin.199120192
Autor:
L. N. Yakhontov, A. V. Denisov, V. A. Azimov, V. P. Morgalyuk, M. D. Mashkovskii, V. A. Bondarenko, S. D. Yuzhakov
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e911908952847af55ac7ccd54225d0
https://doi.org/10.1002/chin.199121192
https://doi.org/10.1002/chin.199121192
Publikováno v:
Pharmaceutical Chemistry Journal. 26:191-209
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::739284176b6d7394cdeaca711a443b07
https://doi.org/10.1007/bf00772931
https://doi.org/10.1007/bf00772931
Autor:
K. F. Turchin, Yu. N. Sheinker, L. N. Yakhontov, E. F. Kuleshova, M. F. Marshalkin, G. P. Zhichareva
Publikováno v:
Pharmaceutical Chemistry Journal. 25:22-26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e2d26f35d851393e84e2b9eeffad13b
https://doi.org/10.1007/bf00766360
https://doi.org/10.1007/bf00766360
Publikováno v:
Chemistry of Heterocyclic Compounds. 26:1375-1383
Using the example of the reaction of 1,3,5-triazines simultaneously containing trichloromethyl and ethoxycarbonyl substituents with phenylhydrazine, it was shown that the presence of even one ester group leads to ring transformation. Depending on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af030509fb171ad8eaaf1fa10386cac8
https://doi.org/10.1007/bf00473967
https://doi.org/10.1007/bf00473967